Canonical Allele Identifier: CA200385314
Gene: PKN3 HGNC NCBI

Linked Data

dbSNP Id: rs72758841
gnomAD v2: 9-131475583-G-C
gnomAD v3: 9-128713304-G-C
gnomAD v4: 9-128713304-G-C
MyVariant Identifiers: chr9:g.131475583G>C (hg19) chr9:g.128713304G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128713304G>C , CM000671.2:g.128713304G>C GRCh38
NC_000009.11:g.131475583G>C , CM000671.1:g.131475583G>C GRCh37
NC_000009.10:g.130515404G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000291906.5:c.1009G>C MANE Select ENSP00000291906.4:p.Asp337His
ENST00000291906.4:c.1009G>C ENSP00000291906.4:p.Asp337His
ENST00000483521.1:n.109G>C
NM_013355.3:c.1009G>C NP_037487.2:p.Asp337His
XM_005251946.3:c.1000G>C XP_005252003.1:p.Asp334His
XM_006717080.2:c.1030G>C XP_006717143.1:p.Asp344His
XM_006717082.2:c.1009G>C XP_006717145.1:p.Asp337His
XM_011518595.1:c.1039G>C XP_011516897.1:p.Asp347His
XM_011518596.1:c.1018G>C XP_011516898.1:p.Asp340His
XM_011518597.1:c.1009G>C XP_011516899.1:p.Asp337His
XM_011518598.1:c.1039G>C XP_011516900.1:p.Asp347His
NM_001317926.1:c.1009G>C NP_001304855.1:p.Asp337His
NM_013355.4:c.1009G>C NP_037487.2:p.Asp337His
XM_006717080.3:c.1030G>C XP_006717143.1:p.Asp344His
XM_017014649.2:c.1030G>C XP_016870138.1:p.Asp344His
XM_017014650.1:c.631G>C XP_016870139.1:p.Asp211His
NM_013355.5:c.1009G>C MANE Select NP_037487.2:p.Asp337His
NM_001317926.2:c.1009G>C NP_001304855.1:p.Asp337His
Search 100 bp 5'
Search 100 bp 3'